Linshang Chemical
PRODUCTS
2,4-Dichloro-1-Nitrobenzene
Linshang Chemical
|
HS Code |
192107 |
| Chemical Formula | C6H3Cl2NO2 |
| Molar Mass | 192.00 g/mol |
| Appearance | Yellow - to - light - brown solid |
| Odor | Characteristic odor |
| Melting Point | 52 - 54 °C |
| Boiling Point | 246 - 248 °C |
| Density | 1.556 g/cm³ (at 20 °C) |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in many organic solvents like benzene, toluene |
| Vapor Pressure | Low vapor pressure |
As an accredited 2,4-Dichloro-1-Nitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,4 - dichloro - 1 - nitrobenzene: Packed in 50 - kg drums for secure storage and transport. |
| Storage | 2,4 - Dichloro - 1 - nitrobenzene should be stored in a cool, dry, well - ventilated area, away from heat sources and ignition points. Keep it in tightly sealed containers to prevent leakage. Store it separately from oxidizing agents, reducing agents, and other incompatible substances to avoid potential chemical reactions. Use appropriate storage cabinets or areas designated for hazardous chemicals. |
| Shipping | 2,4 - Dichloro - 1 - nitrobenzene is shipped in sealed, corrosion - resistant containers. It must be transported in accordance with hazardous chemical regulations, ensuring proper handling to prevent spills and environmental contamination. |
Competitive 2,4-Dichloro-1-Nitrobenzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
We will respond to you as soon as possible.
Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy 2,4-Dichloro-1-Nitrobenzene in China?
As a trusted 2,4-Dichloro-1-Nitrobenzene manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery.
Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
As a leading 2,4-Dichloro-1-Nitrobenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What are the main uses of 2,4-dichloro-1-nitrobenzene?
2% 2C4-dihydro-1-naphthyl methanol has a wide range of uses. In the field of medicine, it is often a key intermediate for the synthesis of many drugs. Due to its unique chemical properties and spatial configuration, this structure can interact with specific targets in organisms to help build molecular structures with specific pharmacological activities. For example, when developing certain cardiovascular diseases, the structure of 2% 2C4-dihydro-1-naphthyl methanol can be introduced to optimize the binding ability of drugs to receptors and improve efficacy.
In the field of materials science, it also has important applications. It can participate in the synthesis of polymer materials and endow materials with special properties by virtue of its own structure. For example, when preparing polymers with specific optical properties, introducing 2% 2C4-dihydro-1-naphthyl methanol as a monomer or modifier can make the material exhibit unique photoluminescence or light absorption properties, which can be used in optical sensors, Light Emitting Diodes and other fields.
In addition, in organic synthetic chemistry, it is a crucial synthetic building block. Chemists can construct more complex and diverse organic compounds by performing various chemical reactions on them, such as oxidation, substitution, addition, etc., providing rich raw materials and pathways for the development of organic synthetic chemistry, and promoting the progress of new compound creation and organic synthesis methodologies.
In the field of materials science, it also has important applications. It can participate in the synthesis of polymer materials and endow materials with special properties by virtue of its own structure. For example, when preparing polymers with specific optical properties, introducing 2% 2C4-dihydro-1-naphthyl methanol as a monomer or modifier can make the material exhibit unique photoluminescence or light absorption properties, which can be used in optical sensors, Light Emitting Diodes and other fields.
In addition, in organic synthetic chemistry, it is a crucial synthetic building block. Chemists can construct more complex and diverse organic compounds by performing various chemical reactions on them, such as oxidation, substitution, addition, etc., providing rich raw materials and pathways for the development of organic synthetic chemistry, and promoting the progress of new compound creation and organic synthesis methodologies.
What are the physical properties of 2,4-dichloro-1-nitrobenzene?
2% 2C4-dihydro-1-naphthylbenzene is one of the organic compounds. Its physical properties are very important and are related to many properties of this substance.
This compound has a specific melting point and boiling point. The melting point is the temperature at which the substance changes from solid to liquid. It has been experimentally determined that the melting point of 2% 2C4-dihydro-1-naphthylbenzene is within a certain range, and this melting point value is of key significance for its purification, identification and application under specific conditions. When at the melting point temperature, the solid 2% 2C4-dihydro-1-naphthylbenzene molecule is energized, and the lattice structure gradually disintegrates, and then converts into a liquid state.
The boiling point is also an important physical property. The boiling point is the temperature at which a substance changes from liquid to gaseous. The boiling point of 2% 2C4-dihydro-1-naphthylbenzene reflects the difficulty of gasification under a certain pressure. When it reaches the boiling point, a large number of bubbles form in the liquid and rise and escape, and the substance completes the transition from liquid to gaseous state. By controlling the temperature and pressure, the boiling point characteristics can be used to separate and purify 2% 2C4-dihydro-1-naphthylbenzene.
Furthermore, its solubility cannot be ignored. 2% 2C4-dihydro-1-naphthylbenzene has different solubility in different solvents. In some organic solvents, such as common benzene, toluene, etc., it exhibits good solubility, which can be miscible with each other due to intermolecular forces. In water, its solubility is poor, due to the large difference between the molecular structure and the polarity of water molecules, it is difficult to form an effective interaction. The different solubility has important applications in chemical synthesis, analysis and testing, etc., which can be used to select suitable solvents for reaction, extraction and other operations.
In addition, the density of 2% 2C4-dihydro-1-naphthylbenzene is also one of the physical properties. Density refers to the mass of a substance per unit volume, which can help to distinguish the substance and plays an important role in operations involving volume and mass conversion. By accurately measuring the density, its purity and other information can be further determined.
In terms of appearance, 2% 2C4-dihydro-1-naphthylbenzene usually appears in a specific form, either crystalline or powdered. The appearance characteristics are also one of the important basis for identifying this compound.
This compound has a specific melting point and boiling point. The melting point is the temperature at which the substance changes from solid to liquid. It has been experimentally determined that the melting point of 2% 2C4-dihydro-1-naphthylbenzene is within a certain range, and this melting point value is of key significance for its purification, identification and application under specific conditions. When at the melting point temperature, the solid 2% 2C4-dihydro-1-naphthylbenzene molecule is energized, and the lattice structure gradually disintegrates, and then converts into a liquid state.
The boiling point is also an important physical property. The boiling point is the temperature at which a substance changes from liquid to gaseous. The boiling point of 2% 2C4-dihydro-1-naphthylbenzene reflects the difficulty of gasification under a certain pressure. When it reaches the boiling point, a large number of bubbles form in the liquid and rise and escape, and the substance completes the transition from liquid to gaseous state. By controlling the temperature and pressure, the boiling point characteristics can be used to separate and purify 2% 2C4-dihydro-1-naphthylbenzene.
Furthermore, its solubility cannot be ignored. 2% 2C4-dihydro-1-naphthylbenzene has different solubility in different solvents. In some organic solvents, such as common benzene, toluene, etc., it exhibits good solubility, which can be miscible with each other due to intermolecular forces. In water, its solubility is poor, due to the large difference between the molecular structure and the polarity of water molecules, it is difficult to form an effective interaction. The different solubility has important applications in chemical synthesis, analysis and testing, etc., which can be used to select suitable solvents for reaction, extraction and other operations.
In addition, the density of 2% 2C4-dihydro-1-naphthylbenzene is also one of the physical properties. Density refers to the mass of a substance per unit volume, which can help to distinguish the substance and plays an important role in operations involving volume and mass conversion. By accurately measuring the density, its purity and other information can be further determined.
In terms of appearance, 2% 2C4-dihydro-1-naphthylbenzene usually appears in a specific form, either crystalline or powdered. The appearance characteristics are also one of the important basis for identifying this compound.
What are the chemical properties of 2,4-dichloro-1-nitrobenzene?
2% 2C4-difluoro-1-methoxybenzene is an organic compound. Its chemical properties are as follows:
In this compound, fluorine atoms and methoxy groups have a great influence on its chemical properties. Fluorine atoms have strong electronegativity, which can reduce the electron cloud density of the benzene ring, and the electrophilic substitution activity of the benzene ring is different from that of the ordinary benzene ring. For example, in the electrophilic substitution reaction such as halogenation reaction and nitrification reaction, its reactivity may be lower than that of benzene. And because of the strong electronegativity of fluorine atoms, the electron cloud density of the ortho and para-sites will be reduced even more than that of the sites. Therefore, the electrophilic reagents may be more likely to attack the meso-sites, and the product distribution is different from that of conventional The electron cloud density of the benzene ring can be increased by methoxy group, which can check and balance the interaction with fluorine atoms. The electron cloud density of the benzene ring can be increased by the electron conjugation effect of methoxy group, which may improve the electrophilic substitution activity of the benzene ring to a certain extent, especially under certain reaction conditions, or guide the electrophilic reagents to attack the ortho and para-sites.
In the redox reaction, the benzene ring of 2% 2C4-difluoro-1-methoxylbenzene is difficult to be oxidized because of its relatively stable structure. However, in the case of strong oxidizing agents, the electron cloud density distribution of the benzene ring may cause oxidation reactions at specific locations, depending on the reaction conditions and the type of oxidizing agent. As for the reduction reaction, if there is a suitable reducing agent, the phenyl ring or can be partially hydrogenated and reduced, or the methoxy group may also participate in the reaction and undergo demethylation and other changes.
When reacting with other reagents, the fluorine atom of the compound can participate in the nucleophilic substitution reaction. Although the carbon-fluorine bond energy is high, under certain conditions, such as high temperature, strong base or specific catalyst, the fluorine atom may be replaced by other nucleophilic reagents to form a new organic compound. The oxygen atom of the methoxy group has lone pair electrons, or participates in the reaction as a nucleophilic check point, and undergoes nucleophilic substitution with reagents such as halogenated hydrocarbons to form new ether compounds. In conclusion, 2% 2C4-difluoro-1-methoxybenzene is rich in chemical properties and has important applications in the field of organic synthesis.
In this compound, fluorine atoms and methoxy groups have a great influence on its chemical properties. Fluorine atoms have strong electronegativity, which can reduce the electron cloud density of the benzene ring, and the electrophilic substitution activity of the benzene ring is different from that of the ordinary benzene ring. For example, in the electrophilic substitution reaction such as halogenation reaction and nitrification reaction, its reactivity may be lower than that of benzene. And because of the strong electronegativity of fluorine atoms, the electron cloud density of the ortho and para-sites will be reduced even more than that of the sites. Therefore, the electrophilic reagents may be more likely to attack the meso-sites, and the product distribution is different from that of conventional The electron cloud density of the benzene ring can be increased by methoxy group, which can check and balance the interaction with fluorine atoms. The electron cloud density of the benzene ring can be increased by the electron conjugation effect of methoxy group, which may improve the electrophilic substitution activity of the benzene ring to a certain extent, especially under certain reaction conditions, or guide the electrophilic reagents to attack the ortho and para-sites.
In the redox reaction, the benzene ring of 2% 2C4-difluoro-1-methoxylbenzene is difficult to be oxidized because of its relatively stable structure. However, in the case of strong oxidizing agents, the electron cloud density distribution of the benzene ring may cause oxidation reactions at specific locations, depending on the reaction conditions and the type of oxidizing agent. As for the reduction reaction, if there is a suitable reducing agent, the phenyl ring or can be partially hydrogenated and reduced, or the methoxy group may also participate in the reaction and undergo demethylation and other changes.
When reacting with other reagents, the fluorine atom of the compound can participate in the nucleophilic substitution reaction. Although the carbon-fluorine bond energy is high, under certain conditions, such as high temperature, strong base or specific catalyst, the fluorine atom may be replaced by other nucleophilic reagents to form a new organic compound. The oxygen atom of the methoxy group has lone pair electrons, or participates in the reaction as a nucleophilic check point, and undergoes nucleophilic substitution with reagents such as halogenated hydrocarbons to form new ether compounds. In conclusion, 2% 2C4-difluoro-1-methoxybenzene is rich in chemical properties and has important applications in the field of organic synthesis.
What is the production method of 2,4-dichloro-1-nitrobenzene?
The preparation method of 2% 2C4-dihydro-1-naphthyl ketone is as follows:
First, take an appropriate amount of naphthalene, place it in the reaction kettle, add a specific catalyst, add an appropriate amount of hydrogen, and control the temperature to a suitable range to hydrogenate the naphthalene to obtain 2,4-dihydronaphthalene. This step requires attention to the flow rate, reaction temperature and time of hydrogen to avoid excessive hydrogenation or insufficient reaction.
Then, take 2,4-dihydronaphthalene, react with an appropriate amount of acylating reagent, such as acetyl chloride or acetic anhydride, catalyzed by Lewis acid catalyst, and react at the appropriate temperature. During the process, the proportion of reactants, reaction temperature and time are carefully adjusted to promote the acylation reaction to proceed fully to generate 2% 2C4-dihydro-1-naphthyl ketone. After the reaction is completed, the product is purified by distillation, extraction, recrystallization, etc. to obtain a high-purity product.
During distillation, according to the boiling point characteristics of 2% 2C4-dihydro-1-naphthyl ketone, the crude product is precisely controlled and separated. In the extraction step, the appropriate extractant is selected to effectively extract the product from the reaction system. The appropriate solvent is selected for recrystallization to allow the product to crystallize and precipitate under suitable conditions to remove impurities and improve purity. Thus, through a series of steps, the target product 2% 2C4-dihydro-1-naphthyl ketone can be obtained.
First, take an appropriate amount of naphthalene, place it in the reaction kettle, add a specific catalyst, add an appropriate amount of hydrogen, and control the temperature to a suitable range to hydrogenate the naphthalene to obtain 2,4-dihydronaphthalene. This step requires attention to the flow rate, reaction temperature and time of hydrogen to avoid excessive hydrogenation or insufficient reaction.
Then, take 2,4-dihydronaphthalene, react with an appropriate amount of acylating reagent, such as acetyl chloride or acetic anhydride, catalyzed by Lewis acid catalyst, and react at the appropriate temperature. During the process, the proportion of reactants, reaction temperature and time are carefully adjusted to promote the acylation reaction to proceed fully to generate 2% 2C4-dihydro-1-naphthyl ketone. After the reaction is completed, the product is purified by distillation, extraction, recrystallization, etc. to obtain a high-purity product.
During distillation, according to the boiling point characteristics of 2% 2C4-dihydro-1-naphthyl ketone, the crude product is precisely controlled and separated. In the extraction step, the appropriate extractant is selected to effectively extract the product from the reaction system. The appropriate solvent is selected for recrystallization to allow the product to crystallize and precipitate under suitable conditions to remove impurities and improve purity. Thus, through a series of steps, the target product 2% 2C4-dihydro-1-naphthyl ketone can be obtained.
What are the environmental effects of 2,4-dichloro-1-nitrobenzene?
2% 2C4-difluoro-1-methoxybenzene, the impact of this substance on the environment is quite complex.
It is volatile, escapes in the atmosphere, or reacts photochemically with other chemicals, which in turn affects the composition and quality of the atmosphere. If it enters the water body, due to its chemical properties, it may not be soluble in water, but it may be attached to suspended particles, which are ingested by aquatic organisms, transmitted and enriched through the food chain, threatening the balance of aquatic ecosystems. In the soil, it may affect the activity of soil microorganisms and soil fertility, inhibit plant growth, change plant physiological metabolism, cause abnormal development, and affect crop yield and quality.
And the chemical properties of this substance may be relatively stable. It degrades slowly in the environment, is easy to remain for a long time, and accumulates continuously, causing lasting pressure on the environment. When the fluorine element it contains participates in environmental chemical processes, it may change the chemical behavior and ecological effects of the substance. In organisms, it may interfere with biological enzyme activities and cell metabolism, posing a latent risk to the health of organisms.
From this perspective, the impact of 2% 2C4-difluoro-1-methoxybenzene on the environment is multi-faceted and far-reaching. It needs to be treated with caution, and monitoring and control should be strengthened to ensure the well-being of the ecological environment.
It is volatile, escapes in the atmosphere, or reacts photochemically with other chemicals, which in turn affects the composition and quality of the atmosphere. If it enters the water body, due to its chemical properties, it may not be soluble in water, but it may be attached to suspended particles, which are ingested by aquatic organisms, transmitted and enriched through the food chain, threatening the balance of aquatic ecosystems. In the soil, it may affect the activity of soil microorganisms and soil fertility, inhibit plant growth, change plant physiological metabolism, cause abnormal development, and affect crop yield and quality.
And the chemical properties of this substance may be relatively stable. It degrades slowly in the environment, is easy to remain for a long time, and accumulates continuously, causing lasting pressure on the environment. When the fluorine element it contains participates in environmental chemical processes, it may change the chemical behavior and ecological effects of the substance. In organisms, it may interfere with biological enzyme activities and cell metabolism, posing a latent risk to the health of organisms.
From this perspective, the impact of 2% 2C4-difluoro-1-methoxybenzene on the environment is multi-faceted and far-reaching. It needs to be treated with caution, and monitoring and control should be strengthened to ensure the well-being of the ecological environment.
Scan to WhatsApp
